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GLRA1 抗体 (AA 29-154)

GLRA1 适用: 人 WB, ELISA, IHC, ICC, FACS, Neut 宿主: 小鼠 Monoclonal 7F8E2 unconjugated
产品编号 ABIN5611339
发货至: 中国
  • 抗原 See all GLRA1 抗体
    GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
    抗原表位
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 29-154
    适用
    • 30
    • 16
    • 15
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 27
    • 3
    • 1
    小鼠
    克隆类型
    • 27
    • 3
    单克隆
    标记
    • 20
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GLRA1 antibody is un-conjugated
    应用范围
    • 19
    • 11
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunocytochemistry (ICC), Flow Cytometry (FACS), Neutralization (Neut)
    纯化方法
    purified
    免疫原
    Purified recombinant fragment of human GLRA1 (AA: extra 29-154) expressed in E. coli.
    克隆位点
    7F8E2
    亚型
    IgG1
    Top Product
    Discover our top product GLRA1 Primary Antibody
  • 应用备注
    ELISA: 1:10000, WB: 1:500 - 1:2000, ICC: N/A, FCM: N/A, IHC: N/A
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified antibody in PBS with 0.05 % sodium azide
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C/-20 °C
    储存方法
    4°C, -20°C for long term storage
  • 抗原
    GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
    别名
    GLRA1 (GLRA1 产品)
    别名
    GLYRA1 antibody, HKPX1 antibody, STHE antibody, [a]Z1 antibody, B230397M16Rik antibody, nmf11 antibody, oscillator antibody, ot antibody, spasmodic antibody, spd antibody, glycine receptor alpha 1 antibody, glycine receptor, alpha 1 antibody, glycine receptor, alpha 1 subunit antibody, GLRA1 antibody, Glra1 antibody, glra1 antibody
    背景

    Description: The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Multiple transcript variants encoding different isoforms have been found.

    Aliases: STHE, HKPX1

    分子量
    52.6 kDa
    基因ID
    2741
    HGNC
    2741
    途径
    Synaptic Membrane
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